Cannabis plant named ‘DKJ127’

ABSTRACT

‘DKJ127’ is a Cannabis sativa cultivar suitable for production of herbal medicinal products (standardized extract) having high to very high THC content, about 17-20% THC eq.

Latin name of the genus and species: The Latin name of the novel plantcultivar disclosed herein is Cannabis sativa (L.).

Variety denomination: This new and distinct cultivar of Cannabis saliva(L.) has been given the denomination ‘DKJ127’.

STATEMENT OF PRIORITY

This application claims the benefit, under 35 U.S.C. § 119 (a-c), ofEuropean Community Plant Variety Application No. 2021/3223 filed on Dec.9, 2021, the entire contents of which is incorporated by referenceherein.

BACKGROUND OF THE INVENTION

Cannabis sativa is indigenous to Central Asia, and South Asia and haslong been used for fiber (hemp), seed and seed oils, for medicinalpurposes, and as a recreational drug. The present invention is directedto a new and distinct Cannabis sativa cultivar named ‘DKJ127’ having ahigh level of THC, a low degree of variation in chemical profile and lowsusceptibility to diseases, and which is suitable for further processinginto a standardized medicinal product.

Lineage, Cultivation, and Selection.

A parental “motherplant” for ‘DKJ127’ was originally selected from seedof the Cannabis strain ‘Jack Herer’ using phenotype selection. Due toits complex lineage, seed of the ‘Jack Herer’ strain is known to displaymany different phenotypes and does not produce uniform plants.Therefore, phenotype selection was initiated to develop a suitableparental motherplant having the desirable phenotype, which was thenfurther propagated via cuttings to show that the characteristics of theselected candidate variety as described are stable over differentpropagation generations.

For selection of the variety ‘DKJ127’, two hundred ‘Jack Herer’ seedswere individually grown under unique cultivation/environmentalconditions (see, Table 1), and a stock of motherplants was created bytaking cuttings from the plants grown from each of the 200 ‘Jack Herer’seeds. The selection criteria for the specific genetics and phenotypesof the seed grown plants included the successful germination of the seed(must germinate), successful cultivation of the motherplant through thevegetative and flowering phases, the rooting behaviour of cuttings(successful rooting), yield (flower size), the resistance to diseases,such as grey mould, and a tetrahydrocannabinolic acid (THCA) content ofat least 15%.

The motherplants start as cuttings in 4×4 cm rockwool cubes, which arethen transplanted three weeks later into 20×20 cm rockwool cubes. Thelifetime of a motherplant is between 8 and 12 months, after which it isdiscarded. During its lifetime, a motherplant can deliver cuttings everysecond week, starting from week 8 of its life. Every time after takingcuttings, the motherplants are trimmed and shaped. Cuttings are grown inan 18-hour day light cycle with a 6-hour night period. Total time invegetative stage is 2 weeks.

To induce flowering, the period of light is shortened to 12 h/day andthe nutrient recipe is switched to a higher potassium and phosphorusblend to promote development of the flowers. The plants are pruned about10 days after starting induction for flowering. Pruning removesunnecessary leaves and branches from the lower side of the plant toallow light to reach all flowers. The period of flowering stage forDKJ127 is about 9 weeks after which flowers are harvested. Starting from30-40 cm height, the plants can reach up to 140 cm-150 cm in height, atthe end of the flowering stage.

As part of the selection process, batch-to-batch consistency wasanalyzed based on the cannabinoid and terpene profile. ‘DKJ127’ containsTHCA at a content of approximately 18% and this high level of THCA wasobserved batch to batch for ‘DKJ127’. Only small amounts of othercannabinoids are present in ‘DK-J127’, mainly Cannabigerol (CBG) andCannabidiol (CBD) at a content of about 0.7% and 0.2%. No othercannabinoids are present in ‘DKJ127’ in significant amounts. The majorterpenes found in ‘DK-J127’ include alpha-pinene, camphene, beta-pinene,beta-myrcene, d-limonene, linalool, beta-caryophyllene, alpha-humulene,nerolidol, guaiol, and alpha-bisabolol.

Environmental conditions:

TABLE 1 Environmental Conditions Cultivation Phases AIR- AIR-Rel.AIR-CO2 LIGHT- Phase/ temperature Humidity Level daylength Parameter (°C.) (%) (ppm) (hours) Rooting Phase 25-29 n/a 500-800 18 Vegetative22-28 60-80 500-800 18 Phase Flowering 22-28 30-50  500-1000 12 Phase

Table 2 and Table 3 below provide data used in the selection process.

TABLE 2 THCA and percent weight loss on drying of 22 selected strainsLoss on drying Strain-ID % (w/w) THCA DK-J120-000 5% 23.80% DK-J127-0005% 21.70% DK-J019-000 5% 21.60% DK-J115-000 6% 20.50% DK-J064-000 5%20.30% DK-J087-000 5% 20.10% DK-J002-000 5% 19.60% DK-J186-000 5% 19.10%DK-J140-000 5% 18.20% DK-J168-000 6% 17.90% DK-J176-000 5% 17.90%DK-J149-000 5% 17.80% DK-J105-000 6% 17.60% DK-J187-000 6% 17.50%DK-J039-000 7% 17.40% DK-J166-000 6% 17.20% DK-J093-000 6% 16.80%DK-J024-000 6% 16.60% DK-J085-000 7% 16.50% DK-J110-000 5% 16.50%DK-J033-000 5% 15.70% DK-J099-000 7% 12.40%

TABLE 3 Yield and cultivation behaviour and THC content wt wt seedsmaturity Strain- ht wet dry in level ID [cm] [g] [g] Factor flowers[1-10] DK- 155 260 60.25 4.3 no 8 J002 DK- 175 600 133.2 4.5 no 9 J003DK- 165 440 74.8 5.9 no 7 J019 DK- 176 740 142.35 5.2 no 8 J024 DK- 180480 105 4.6 no 7 J033 DK- 180 1460 369.92 3.9 yes 8 J039 DK- 200 860193.6 4.4 no 9 J064 DK- 165 620 136.8 4.5 no 8 J085 DK- 175 580 131.894.4 no 9 J087 DK- 150 220 43.63 5.0 no 7 J088 DK- 155 2000 417.31 4.8 no7 J093 DK- 170 500 107.79 4.6 no 7 J099 DK- 170 1040 216.14 4.8 no 8J105 DK- 130 1220 205.13 5.9 no 7 J110 DK- 200 1020 212.83 4.8 no 9 J115DK- 180 840 193.27 4.3 no 9 J127 DK- 160 1120 214.79 5.2 no 7 J130 DK-170 620 146.22 4.2 no 8 J140 DK- 200 840 186.4 4.5 no 7 J149 DK- 180 42098.35 4.3 no 8 J166 DK- 184 1120 236.56 4.7 no 8 J186 DK- 185 1060286.38 3.7 no 8 J187 rooting rooting THC Strain- rooting test 1 test 2eq. ID disease time [20] [11] [%] DK- no 10-18 20 11 19.6% J002 days DK-no 10-18 20 10 NA J003 days DK- no 10-18 19 11 21.6% J019 days DK- no10-18 6 7 16.6% J024 days DK- no 10-18 20 11 15.7% J033 days DK- no10-18 17 11 17.4% J039 days DK- no 10-18 20 11 20.3% J064 days DK- no10-18 20 11 16.5% J085 days DK- no 10-18 20 11 20.1% J087 days DK- no10-18 6 11 NA J088 days DK- no 10-18 5 11 16.8% J093 days DK- no 10-1820 11 12.4% J099 days DK- no 10-18 20 11 17.6% J105 days DK- no 10-18 1011 16.5% J110 days DK- no 10-18 20 11 20.5% J115 days DK- no 10-18 19 1121.7% J127 days DK- grey 10-18 10 11 NA J130 mould days DK- no 10-18 2011 18.2% J140 days DK- no 10-18 5 11 17.8% J149 days DK- no 10-18 20 1117.2% J166 days DK- no 10-18 20 11 19.1% J186 days DK- no 10-18 10 1117.5% J187 days

In summary, out of 200 ‘Jack Herer’ seedlings, 22 were selected forfurther analysis and asexual reproduction via cuttings. These 22phenotypes were brought into the flowering phase and material of thosewas dried and analyzed for THCA content. The content of THCA, terpeneprofile and odour were included as criteria in the selection of the linenamed J127 (DK-J127-000) (‘DKJ127’). Thus, from an initial group of 200‘Jack Herer’ seedlings, exhibiting a wide range of phenotypes, a singlestrain, ‘DKJ127’, having the desired and true to type characteristics asdescribed herein was selected.

Although ‘Jack Herer’, due to its complex lineage, is known to be astrain that displays many different phenotypes, the applicant has nowdeveloped a plant that shows stability over multiple propagationgenerations.

The detailed steps of cultivation and conditions for the initialmotherplants from seeds is described as follows:

Two hundred ‘Jack Herer’ seeds were individually grown under uniquecultivation conditions and motherplants were created.

Step 1: Preparation of rockwool cubes (4.0×4.0×4.0 cm) with tap water.

Step 2: Transplantation of seed onto the rockwool cube.

Step 3: Seed covered by rockwool, about 1 cm deep.

Step 4: Rockwool cube placed under a white plastic foil tent.

Step 5: Seed germinates after 3-14 days underneath the white plasticfoil tent.

Step 6: Evaluation of whether the selection criteria have been met.

Step 7: Transplantation of seedling in rockwool cubes (20×20×20 cm).

Step 8: Soaking with Fertilizer with EC 0.5-3.5 and pH value of 4.5-7.

Step 9: Cultivation period of plants before initial propagation bytaking cuttings is 3-6 weeks.

Step 10: Plants are kept in same conditions with daily watering andincrease of light intensity up to specifications for plants inVegetative Phase.

The detailed steps of cultivation of motherplants by cuttings isdescribed as follows:

Step 1: Soaking of rockwool cubes (4.0×4.0×4.0 cm) in fertilizers withan EC value of 1.4±0.2 mS/cm and a pH value of 5.5-6.5 includingnematodes (Steinernema feltiae) for a minimum of 10 minutes.

Step 2: Taking a cutting of approximately 8-12 cm and 2-3 unfoldedleaves of the motherplant.

Step 3: Removing of lower leaves of the cutting.

Step 4: Cutting the stem at the lower end with an angle of 45 degrees.

Step 5: Cutting in half the upper large leaves.

Step 6: Removing the uppermost layer (approximately 2 mm) of the stem ofthe lower 2 cm of the step.

Step 7: Sticking of cutting in the prepared rockwool cubes with a depthof approximately 1.5-2 cm.

Step 8: Placing of the cutting sticking in the rockwool cubed under awhite plastic foil tent.

Step 9: Spray the cutting with water to increase the humidity under thewith plastic foil tent.

Step 10: After day 1 the white plastic foil tent is cut open at the topwith holes of approximately 5 cm (1 hole for every m²).

Step 11: In day 3-9 the cuttings are supplied with fertilizer for 15 min(EC 1.4±0.2 mS/cm) by flooding the cultivation table.

Step 12: On day 9±2 further holes are cut in the white plastic tent,approximately 5 cm (5 holes for every m²).

Step 13: Between day 10-13 cuttings are supplied with fertilizer for 15min (EC 1.6±0.2 mS/cm) by flooding the cultivation table.

Step 14: On day 11±2 the white plastic tent is removed for 15-60min/day.

Step 15: On day 14 until Vegetative Phase the cuttings are supplied withfertilizer for 15 min (EC 1.8±0.2 mS/cm by flooding the cultivationtable. In addition, the white plastic tent is replaced with acryl meshfor 1-2 days.

Step 16: For the days until Vegetative Phase (approximately day 21)cuttings are uncovered in greenhouse.

Step 17: Preparation of rockwool cubes for Vegetative Phase (15×15×14.2cm) with the insertion of two to three drippers in each rockwool cube byan 45° angle into the cube.

Step 18: Soaking of the rockwool cubes in fertilizer with EC of 2.2-2.8mS/cm and a pH value 5.5-6.5 by fertilizer from the installed drippersfor 20±5 seconds for 20±5 times, with a 5 min break in between.

Step 19: Soaking of rockwool cubes with fertilizer containing nematodes(Steinernema feltiae) from drippers.

Step 20: Transition from Rooting phase (approx. 21 days) to VegetativePhase (approx. 14 days).

Step 21: Transplantation of cutting in rockwool cubes for VegetativePhase.

Step 22: Plants are kept under the same conditions for their lifetime ofabout 8 to 12 months with fertilizer of 2.2-2.8 mS/cm and a pH value5.5-6.5.

The detailed steps of cultivation of production plants by cuttings isdescribed as follows:

Step 1: Soaking of rockwool cubes (4.0×4.0×4.0 cm) in fertilizers withan EC value of 1.4±0.2 mS/cm and a pH value of 5.5-6.5 includingnematodes (Steinernema feltiae) for a minimum of 10 minutes.

Step 2: Taking a cutting of approximately 8-12 cm and 2-3 unfoldedleaves of the motherplant.

Step 3: Removing of lower leaves of the cutting.

Step 4: Cutting the stem at the lower end with an angle of 45 degrees.

Step 5: Cutting in half the upper large leaves.

Step 6: Removing the uppermost layer (approximately 2 mm) of the stem ofthe lower 2 cm of the step.

Step 7: Sticking of cutting in the prepared rockwool cubes with a depthof approximately 1.5-2 cm.

Step 8: Placing of the cutting sticking in the rockwool cubed under awhite plastic foil tent.

Step 9: Spray the cutting with water to increase the humidity under thewith plastic foil tent.

Step 10: After day 1 the white plastic foil tent is cut open at the topwith holes of approximately 5 cm (1 hole for every m²).

Step 11: In day 3-9 the cuttings are supplied with fertilizer for 15 min(EC 1.4±0.2 mS/cm) by flooding the cultivation table.

Step 12: On day 9±2 further holes are cut in the white plastic tent,approximately 5 cm (5 holes for every m²).

Step 13: Between day 10-13 cuttings are supplied with fertilizer for 15min (EC 1.6±0.2 mS/cm) by flooding the cultivation table.

Step 14: On day 11±2 the white plastic tent is removed for 15-60min/day.

Step 15: On day 14 until Vegetative Phase the cuttings are supplied withfertilizer for 15 min (EC 1.8±0.2 mS/cm by flooding the cultivationtable. In addition, the white plastic tent is replaced with acryl meshfor 1-2 days.

Step 16: For the days until Vegetative Phase (approximately day 21)cuttings are uncovered in greenhouse.

Step 17: Preparation of rockwool cubes for Vegetative Phase (15×15×14.2cm) with the insertion of two to three drippers in each rockwool cube byan 45° angle into the cube.

Step 18: Soaking of the rockwool cubes in fertilizer with EC of 2.2-2.8mS/cm and a pH value 5.5-6.5 by fertilizer from the installed drippersfor 20±5 seconds for 20±5 times, with a 5 min break in between.

Step 19: Soaking of rockwool cubes with fertilizer containing nematodes(Steinernema feltiae) from drippers.

Step 20: Transition from Rooting phase (approx. 21 days) to VegetativePhase (approx. 14 days)

Step 21: Transplantation of cutting in rockwool cubes for VegetativePhase.

Step 22: Until flowering phase plants are supplied with fertilizer for2±1,5 min with an EC value of 2.4±0.2 mS/cm for every day by drippers.

Step 23: Plants are topped after day 7±2 days in Vegetative Phase bycutting the top above 4/6 branches

Step 24: Transition from Vegetative Phase (approx. 14 days) to Floweringphase (approx. 9 weeks)

Step 25: Flowering phase is initiated by changing the daylight from 18h/day to 12 h/day.

Step 26: The plants are supplied with fertilizer during the Floweringphase every day for 3±1 times for 2±1.5 min with EC of 2.2-30 mS/cm.

Step 27: After 10±5 days in flowering removing of all shoots and leavesin the lower half of the plant by directly cutting on the side shoot

Step 28: Remaining flowering phase of approx. 9 weeks

Executing of pest inspection every day in all phases, spreading ofbeneficials as needed (Nematodes, Hypoaspis, Atheta, Orius, AphidiusColemani, Cucumeris, Californicus, Swirskii, Felitiella acarisuja)

Asexual Reproduction.

‘DKJ127’ has been propagated as vegetative stem cuttings since itsoriginal selection. The first propagation of ‘DKJ127’ took place on Aug.1, 2019 at Vertanical Denmark ApS, Birketvedvejen 31, 5290 Marslev,Denmark. The characteristics disclosed herein for ‘DKJ127’ have remainedstable and the plant has reproduced true to type through successivegenerations of asexual propagation.

SUMMARY OF THE INVENTION

‘DK-J12’ is a high THC producing Cannabis cultivar. “DKJ127” representsa significant improvement over existing Cannabis strains in terms of itsunique cannabinoid profile and high yield. The inventive step lies inthe discovery of a specific combination of genetic traits that result inthe desirable characteristics of the strain.

‘DKJ127’ exhibits a high to very high THC content, about 17-20% THC eq.and absent to low CBD content, about 0.07% CBD eq., which characteristicreproduces true to type through successive generations of asexualpropagation and distinguishes ‘DKJ127’ as a new and distinct Cannabiscultivar.

BRIEF DESCRIPTION OF THE DRAWINGS

The photographs in the drawings were made using conventional techniquesand show the colors as true as reasonably possible by conventionalphotography. Colors in the photographs may differ slightly from thecolor values cited in the detailed botanical description, whichaccurately describe the colors of the new Cannabis sativa variety‘DKJ127’. As used herein, the term “variety” is interchangeable with theterms “cultivar,” “line” and/or “strain.”

FIG. 1 is a color photograph of a leaflet of the new cultivar ‘DKJ127’.

FIG. 2 is a color photograph of a stem of the new cultivar ‘DKJ127’.

FIG. 3 is a color photograph of a plant of the new cultivar ‘DKJ127’.

FIGS. 4A and 4B show color photographs of the new cultivar ‘DKJ127’ atdifferent stages of growth. FIG. 4A shows a 5-month-old plant and FIG.4B shows a 7-month-old plant.

FIG. 5 is a color photograph of a cutting of the new cultivar ‘DKJ127’,which is 1.5 weeks old.

FIG. 6 is a color photograph of a plant of the new cultivar ‘DKJ127’ inthe vegetative stage that is 4.5 weeks old.

FIG. 7 is a color photograph of the stem of a plant of the new cultivar‘DKJ127’ that is 7 months old.

FIG. 8 and FIG. 9 are a color photographs of the flower of a plant ofthe new cultivar ‘DKJ127’.

FIG. 10 shows the concentrations of various terpenes from differentbatches of ‘DKJ127’. ‘VER-01-THC’ is the commercial name for ‘DKJ127’.

FIG. 11 shows a bottom flower of ‘DKJ127’.

FIG. 12 shows a middle flower of ‘DKJ127’.

FIG. 13 shows a top flower of ‘DKJ127’.

DETAILED BOTANICAL DESCRIPTION

The following is a detailed description of the botanical characteristicsof a new and distinct cultivar of Cannabis sativa plant given thedesignation ‘DKJ127’. All colors cited herein refer to The RoyalHorticultural Society Colour Chart (The Royal Horticultural Society(R.H.S.), London, 2007 Edition). Where dimensions, sizes, colors, andother characteristics are given, it is to be understood that suchcharacteristics are approximations or averages set forth as accuratelyas practicable.

‘DKJ127’ has not been observed under all possible environmentalconditions; therefore, the phenotype may vary under differentenvironmental conditions such as season, temperature, light intensity,day length, cultural conditions, and the like, without, however, anyvariance in the genotype.

TECHNICAL DESCRIPTION OF THE CULTIVAR

-   Classification.    -   -   Botanical name.—Cannabis saliva (L.).        -   Common name.—Cannabis.        -   Variety name.—‘DKJ127’.-   Parentage: Seedling selection grown from ‘Jack Herer’ seed.-   Propagation: Typically propagated asexually via stem cuttings.-   Plant description:    -   -   Plant height.—Medium; about 140 cm-150 cm by the end of            flowering.-   Main stem:    -   -   Shape.—Strong, erect, woody and coarse. It varies in            thickness, thicker in the bottom, and narrower in the top.        -   Average diameter at the bottom.—1.8-2.5 cm.        -   Average diameter.—1 cm.        -   Average internodal length.—4 cm.        -   Furrow depth.—Shallow.        -   Amount of pith in cross-section.—Absent.        -   Thrycome type.—No trichomes on stem.        -   Color designation.—Green (close to RHS 140 A), with violet            stripes (close to RHS 86A), and grey tones at the bottom            (close to RHS 139 D).-   Foliage:    -   -   Leaf description.—Arrangement: serrate leaflets arranged            alternately on the stems. Size: Length: fluctuates from 5 cm            to 23 cm, depending by age and position (without petiole).            Width: fluctuates from 6 cm to 15 cm depending by age and            position (without petiole). Margin: coarsely serrate.            Trichomes type: non-glandular, cystolithic. Leaflet shape:            broad. Leaflet size (Length and width in cm): 5 cm-23 cm,            similar to ‘Dioca 88’. Average number of leaflets per leaf:            5, similar to ‘Epsilon 68’. Leaf tip: pointed. Base shapes:            obtuse. Color designations of the leaf veins (top surface):            light green (close to RHS 142 D). Color designations of the            leaf veins (bottom surface): light green (close to RHS 142            D). Color specification of the top surface: dark green:            (close to RHS 141B). Color specification of the bottom            surface: green (close to RHS 139A).        -   Petiole description.—Length: fluctuates, from 3 cm to 15 cm,            depending by the age of the leaf and position on the plant            (bottom, mid or top). Anthocyanin staining: medium purple            coloration (close to RHS N77B). Thrycome type: cystolithic            trichomes. Coloring: green (close to RHS: 145A).-   Flower description: The average diameter of DKJ127 flower is 4 cm at    the end of week 9 in flowering phase. It is not possible to directly    compare the flower size with the genetic “Jack Herer” as the genetic    “Jack Herer” displays various phenotypes with different flower    sizes.    -   -   Timing of female flowering.—Early to medium. Female            flowering starts approximately 14 days after beginning of            the flowering induction. Induction starts by changing the            daylength from 18 to 12 hours.        -   Period of flowering.—About 9 weeks.        -   Color.—Dark to bright green, sometimes purple on the upper            part (RHS: 143A and RHS: 141B). Bottom flowers are smaller,            since they are exposed to lower light intensity than flowers            located higher up in the plant. The average diameter is            3 cm. See, FIG. 11 . Middle flowers are bigger than bottom            flowers, since they are exposed to higher light intensity.            The average diameter is 4 cm. See, FIG. 12 . Top flowers are            bigger than the flowers located in the middle or at the            bottom of the plant, since they are exposed to higher light            intensity- The average diameter is 5 cm. See, FIG. 13 .-   Inflorescence: Is formed by arrangement of individual flowers    located around a stem. The stem of the inflorescence is thick and    sturdy, and it supports the weight of the flowers. Each flower is    enclosed in a small, cone-shaped structure.    -   -   Pistils are in the center of each flower.—All flowers are            covered with glandular, capitate-stalked trichomes. The            inflorescence is surrounded by sugar-leaves (bracts).        -   Average number of inflorescences per plant.—110.        -   Average number of flowers per inflorescence.—30. DK-J127            develop male flowers at the beginning of week 8 in flowering            phase.        -   Female flowers per plant.—99.998%.        -   Male flowers per plant.—0.002%.        -   Hermaphrodite per plant.—0%.        -   Average number of flowers per inflorescence.—3.        -   Average inflorescence diameter.—4 cm.        -   Terminal bud shape.—Dense, tightly packed, oval shaped,            green color (close to RHS 143A).-   Bract:    -   -   Average size.—5 mm.        -   Shape.—Small, pear-shaped.        -   Trichome type.—Glandular, capitate stalked.        -   Color.—Green (close to RHS 143A).-   Bracteole:    -   -   Average size.—2 cm.        -   Shape.—Tiny leaves, coarsely serrate, covered with            trichomes.        -   Trichome type.—Glandular, capitate stalked.        -   Color.—Green (close to RHS: 141A).-   Productivity (weight/plant), shipping quality and storage life:    DKJ127 is used as a starting product for the product VER-01-THC (dry    Cannabis flowers), which is used for ethanolic extraction. Yield of    dried Cannabis flowers/plant is approximately 60-80 gr. Storage    conditions 15-25° C. Shelf-life 2 years.-   Plant hardiness zone: Hardiness zone 11 with a range between 40° F.    and 50° F. or +4.4° C. and +10° C.-   Chemical content:    -   -   THC and CBD content.—About 17-20% THC eq. and about 0.07%            CBD eq.        -   Terpene content.—DKJ127 produces alpha-pinene, camphene,            beta-pinene, beta-myrcene, d-limonene, linalool,            beta-caryophyllene, alpha-humulene, nerolidol, guaiol, and            alpha-bisabolol. See, FIG. 5 .

COMPARISON TO ‘JACK HERER’

‘DKJ127’ has a consistently higher THC content than ‘Jack Herer’, about17-20% THC eq.

I claim:
 1. A new and distinct cultivar of Cannabis sativa plant named‘DKJ127’, substantially as illustrated and described herein.